BIRTCHER SWIVEL GRIP LAPAROSCOPIC PROBES & ACCESS.
K-Number: K932779 · 1995-03-21
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Device Summary
Frequently Asked Questions
What is the BIRTCHER SWIVEL GRIP LAPAROSCOPIC PROBES & ACCESS.?
BIRTCHER SWIVEL GRIP LAPAROSCOPIC PROBES & ACCESS. is a medical device that received FDA 510(k) clearance on 1995-03-21. The listed applicant is Birtcher Medical Systems, Inc.. The 510(k) number is K932779.
When did BIRTCHER SWIVEL GRIP LAPAROSCOPIC PROBES & ACCESS. receive FDA 510(k) clearance?
BIRTCHER SWIVEL GRIP LAPAROSCOPIC PROBES & ACCESS. received FDA 510(k) clearance on 1995-03-21, under 510(k) number K932779.
Who is the listed applicant for BIRTCHER SWIVEL GRIP LAPAROSCOPIC PROBES & ACCESS.?
The FDA 510(k) record lists Birtcher Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIRTCHER SWIVEL GRIP LAPAROSCOPIC PROBES & ACCESS.?
The FDA product code for BIRTCHER SWIVEL GRIP LAPAROSCOPIC PROBES & ACCESS. is HET.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Birtcher Medical Systems, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: HET)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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